홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

3-Fluorobenzylamine → HCID 86664548, 화합물

HRID 513288
노트
인쇄 미리보기

반응식

HRID 513288 반응식
Cl[C:2]1[C:7]([C:8]([O:10][CH2:11][CH3:12])=[O:9])=[CH:6][N:5]=[C:4]([Cl:13])[C:3]=1[Cl:14].[F:15][C:16]1[CH:17]=[C:18]([CH:21]=[CH:22][CH:23]=1)[CH2:19][NH2:20].CCN(C(C)C)C(C)C>C(C#N)(C)=O>[Cl:14][C:3]1[C:4]([Cl:13])=[N:5][CH:6]=[C:7]([C:2]=1[NH:20][CH2:19][C:18]1[CH:21]=[CH:22][CH:23]=[C:16]([F:15])[CH:17]=1)[C:8]([O:10][CH2:11][CH3:12])=[O:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 668533-FluorobenzylamineHCID 81531DiisopropylethylamineHCID 79611304,5,6-Trichloronicotinic acid ethyl ester

생성물 1

HCID 86664548HCID 86664548, 화합물수율 97.1%

시약·촉매·용매 1

HCID 694302-Oxopropiononitrile용매

반응 조건

온도
50 °C

실험 절차

To a solution of ethyl 4,5,6-trichloronicotinate (200 mg, 0.78 mmol) in AcCN (1.5 mL) was added 3-fluorobenzylamine (0.108 mL, 0.94 mmol) and DIPEA (0.167 mL, 0.94 mmol). The mixture was stirred at room temperature for 5 h them at 50° C. until the reaction is over. The solution was cooled and concentrated, the resulting residue was diluted with water, the solid was then collected by filtration to give ethyl 5,6-dichloro-4-(3-fluorobenzylamino)nicotinate (260 mg).

후처리

  1. temperatureThe solution was cooled
  2. concentrationconcentrated
  3. additionthe resulting residue was diluted with water
  4. filtrationthe solid was then collected by filtration

출처 및 근거

ORD 기록
ord-669a8ed46d5f43fa8b43cdf0ee69a91d
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09102625B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트